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Basics of Notification and Registration of Medical Devices in Brazil - ANVISA

In this video, we explore the crucial differences between notification and registration of medical devices in Brazil, regulated by ANVISA. 🩺🇧🇷 You'll learn about: -What notifications and registrations are, and when each is required -Medical device risk classifications and how they affect the regulatory process -Criteria and documentation needed for notification and registration -Examples of products that fall into each category -The importance of regulatory compliance for healthcare companies Ideal for medical device manufacturers interested in entering the Brazilian market, this video provides a concise overview of essential regulations and certification processes needed for success. Want to launch your medical device in Brazil? Don't miss this essential guide to compliance and market success! Visit www.brisa.com.br for more information and expert support. 📊🔬 #brisa #brisaadvisors #medicaldevices #anvisa #inmetro #anatel #MD #regulatory #BPOinRA #BrazilianMarket #RegulatoryAffairs #Compliance #Licensing #Acquisition #MedicalProducts #Healthcare #LegalConsulting #Regulation #Legislation #RegulatoryConsulting #SpecializedConsulting #ConsultoriaRegulatória #DispositivosMédicos #MercadoBrasileiro #Aquisição #Saúde #Regulamentação #ProdutosMédicos #ConsultoriaEspecializada #ConsultoriaEmRegulação #ConsultoriaInternacional #ImportConsulting #ConsultoriaEmNormas

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